Association between IQ and FMR1 protein (FMRP) across the spectrum of CGG repeat expansions

Fragile X syndrome, the leading heritable form of intellectual disability, is caused by hypermethylation and transcriptional silencing of large (CGG) repeat expansions (> 200 repeats) in the 5′ untranslated region of the fragile X mental retardation 1 (FMR1) gene. As a consequence of FMR1 gene si...

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Detalles Bibliográficos
Autores principales: Kim, Kyoungmi, Hessl, David, Randol, Jamie L., Espinal, Glenda M., Schneider, Andrea, Protic, Dragana, Aydin, Elber Yuksel, Hagerman, Randi J., Hagerman, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938341/
https://www.ncbi.nlm.nih.gov/pubmed/31891607
http://dx.doi.org/10.1371/journal.pone.0226811

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938341/
https://www.ncbi.nlm.nih.gov/pubmed/31891607
http://dx.doi.org/10.1371/journal.pone.0226811

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